全文获取类型
收费全文 | 38465篇 |
免费 | 16355篇 |
国内免费 | 781篇 |
专业分类
55601篇 |
出版年
2023年 | 150篇 |
2022年 | 424篇 |
2021年 | 961篇 |
2020年 | 2483篇 |
2019年 | 4135篇 |
2018年 | 4185篇 |
2017年 | 4326篇 |
2016年 | 4548篇 |
2015年 | 4732篇 |
2014年 | 4498篇 |
2013年 | 5012篇 |
2012年 | 2932篇 |
2011年 | 2481篇 |
2010年 | 3574篇 |
2009年 | 2303篇 |
2008年 | 1307篇 |
2007年 | 823篇 |
2006年 | 810篇 |
2005年 | 707篇 |
2004年 | 700篇 |
2003年 | 620篇 |
2002年 | 524篇 |
2001年 | 526篇 |
2000年 | 441篇 |
1999年 | 360篇 |
1998年 | 164篇 |
1997年 | 141篇 |
1996年 | 119篇 |
1995年 | 103篇 |
1994年 | 111篇 |
1993年 | 73篇 |
1992年 | 149篇 |
1991年 | 131篇 |
1990年 | 86篇 |
1989年 | 95篇 |
1988年 | 71篇 |
1987年 | 92篇 |
1986年 | 79篇 |
1985年 | 86篇 |
1984年 | 52篇 |
1983年 | 47篇 |
1982年 | 45篇 |
1981年 | 32篇 |
1980年 | 28篇 |
1979年 | 51篇 |
1978年 | 37篇 |
1977年 | 29篇 |
1976年 | 29篇 |
1975年 | 28篇 |
1973年 | 29篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
41.
Transbilayer distribution and mobility of phosphatidylinositol in human red blood cells 总被引:3,自引:0,他引:3
P Bütikofer Z W Lin D T Chiu B Lubin F A Kuypers 《The Journal of biological chemistry》1990,265(27):16035-16038
The present studies describe the distribution of phosphatidylinositol (PI) within the membrane bilayer of the human red blood cell (RBC) as well as its transbilayer mobility. The membrane bilayer distribution was determined by measuring the hydrolysis of PI in the exterior leaflet of the RBC membrane using a PI-specific phospholipase C and by extraction of PI from the exterior leaflet using bovine serum albumin. The transbilayer mobility of PI was measured by following the fate of radiolabeled PI which was first incorporated into the outer leaflet of the RBC membrane. Our results indicate that PI is asymmetrically distributed in the membrane, with approximately 80% located in the inner and 20% in the outer leaflet of the bilayer. The rate of transbilayer mobility of PI is similar to that for certain molecular species of phosphatidylcholine and much slower than that reported for the aminophospholipids in the RBC membrane. 相似文献
42.
43.
44.
Monty Krieger Richard G. W. Anderson Joseph L. Goldstein Michael S. Brown Louis C. Smith Yin J. Kao Henry J. Pownall Antonio M. Gotto 《Journal of cellular biochemistry》1979,10(4):467-478
Previous studies have shown that the cholesteryl ester core of plasma low density lipoprotein (LDL) can be extracted with heptane and replaced with a variety of hydrophobic molecules. In the present report we use this reconstitution technique to incorporate two fluorescent probes, 3-pyrenemethyl-23, 24-dinor-5-cholen-22-oate-3β-yl oleate (PMCA oleate) and dioleyl fluorescein, into heptane-extracted LDL. Both fluorescent lipoprotein preparations were shown to be useful probes for visualizing the receptor-mediated endocytosis of LDL in cultured human fibroblasts. When normal fibroblasts were incubated at 37°C with either of the fluorescent LDL preparations, fluorescent granules accumulated in the perinuclear region of the cell. In contrast, fibroblasts from patients with the homozygous form of familial hypercholesterolemia (FH) that lack functional LDL receptors did not accumulate visible fluorescent granules when incubated with the fluorescent reconstituted LDL. A fluorescence-activated cell sorter was used to quantify the fluorescence intensity of individual cells that had been incubated with LDL reconstituted with dioleyl fluorescein. With this technique a population of normal fibroblasts could be distinguished from a population of FH fibroblasts. The current studies demonstrate the feasibility of using fluorescent reconstituted LDL in conjunction with the cell sorter to isolate mutant cells lacking functional LDL receptors. 相似文献
45.
J C Shih R H Chiu Y L Chan 《Biochemical and biophysical research communications》1976,68(4):1348-1355
Some properties of histidine:pyruvate transaminase (HPT) and phenylalanine:pyruvate transaminase (PPT) in the cytosol of rat liver were studied. HPT and PPT activity could not be separated by DEAE-Sephadex A-50 or hydroxylapatite column chromatography, and the ratio of activity remained constant during these purification procedures. The two enzyme activities also showed similar heat stability and responses to glucagon injection. Based on these findings, we suggest that a single enzyme may specifically catalyze histidine:pyruvate and phenylalanine:pyruvate transamination. 相似文献
46.
47.
Lihua Qu Yi Li Chao Chen Tong Yin Qian Fang Yijin Zhao Wenting Lv Ziqi Liu Yangye Chen Li Shen 《Cell death & disease》2022,13(8)
Acute lung injury (ALI) is a potentially life-threatening, devastating disease with an extremely high rate of mortality. The underlying mechanism of ALI is currently unclear. In this study, we aimed to confirm the hub genes associated with ALI and explore their functions and molecular mechanisms using bioinformatics methods. Five microarray datasets available in GEO were used to perform Robust Rank Aggregation (RRA) to identify differentially expressed genes (DEGs) and the key genes were identified via the protein-protein interaction (PPI) network. Lipopolysaccharide intraperitoneal injection was administered to establish an ALI model. Overall, 40 robust DEGs, which are mainly involved in the inflammatory response, protein catabolic process, and NF-κB signaling pathway were identified. Among these DEGs, we identified two genes associated with ALI, of which the CAV-1/NF-κB axis was significantly upregulated in ALI, and was identified as one of the most effective targets for ALI prevention. Subsequently, the expression of CAV-1 was knocked down using AAV-shCAV-1 or CAV-1-siRNA to study its effect on the pathogenesis of ALI in vivo and in vitro. The results of this study indicated that CAV-1/NF-κB axis levels were elevated in vivo and in vitro, accompanied by an increase in lung inflammation and autophagy. The knockdown of CAV-1 may improve ALI. Mechanistically, inflammation was reduced mainly by decreasing the expression levels of CD3 and F4/80, and activating autophagy by inhibiting AKT/mTOR and promoting the AMPK signaling pathway. Taken together, this study provides crucial evidence that CAV-1 knockdown inhibits the occurrence of ALI, suggesting that the CAV-1/NF-κB axis may be a promising therapeutic target for ALI treatment.Subject terms: Cell signalling, Respiratory tract diseases 相似文献
48.
Kathy Darragh Gabriela Montejo‐Kovacevich Krzysztof M. Kozak Colin R. Morrison Clarisse M. E. Figueiredo Jonathan S. Ready Camilo Salazar Mauricio Linares Kelsey J. R. P. Byers Richard M. Merrill W. Owen McMillan Stefan Schulz Chris D. Jiggins 《Ecology and evolution》2020,10(9):3895-3918
In many animals, mate choice is important for the maintenance of reproductive isolation between species. Traits important for mate choice and behavioral isolation are predicted to be under strong stabilizing selection within species; however, such traits can also exhibit variation at the population level driven by neutral and adaptive evolutionary processes. Here, we describe patterns of divergence among androconial and genital chemical profiles at inter‐ and intraspecific levels in mimetic Heliconius butterflies. Most variation in chemical bouquets was found between species, but there were also quantitative differences at the population level. We found a strong correlation between interspecific chemical and genetic divergence, but this correlation varied in intraspecific comparisons. We identified “indicator” compounds characteristic of particular species that included compounds already known to elicit a behavioral response, suggesting an approach for identification of candidate compounds for future behavioral studies in novel systems. Overall, the strong signal of species identity suggests a role for these compounds in species recognition, but with additional potentially neutral variation at the population level. 相似文献
49.
Vicky P. Chen Heidi Q. Xie Wallace K. B. Chan K. Wing Leung Gallant K. L. Chan Roy C. Y. Choi Suzanne Bon Jean Massoulié Karl W. K. Tsim 《The Journal of biological chemistry》2010,285(35):27265-27278
Acetylcholinesterase (AChE) is anchored onto cell membranes by the transmembrane protein PRiMA (proline-rich membrane anchor) as a tetrameric globular form that is prominently expressed in vertebrate brain. In parallel, the PRiMA-linked tetrameric butyrylcholinesterase (BChE) is also found in the brain. A single type of AChE-BChE hybrid tetramer was formed in cell cultures by co-transfection of cDNAs encoding AChET and BChET with proline-rich attachment domain-containing proteins, PRiMA I, PRiMA II, or a fragment of ColQ having a C-terminal GPI addition signal (QN-GPI). Using AChE and BChE mutants, we showed that AChE-BChE hybrids linked with PRiMA or QN-GPI always consist of AChET and BChET homodimers. The dimer formation of AChET and BChET depends on the catalytic domains, and the assembly of tetramers with a proline-rich attachment domain-containing protein requires the presence of C-terminal “t-peptides” in cholinesterase subunits. Our results indicate that PRiMA- or ColQ-linked cholinesterase tetramers are assembled from AChET or BChET homodimers. Moreover, the PRiMA-linked AChE-BChE hybrids occur naturally in chicken brain, and their expression increases during development, suggesting that they might play a role in cholinergic neurotransmission. 相似文献
50.